ENST00000544604.7:c.300+20252C>T
MANE Select
|
ENSP00000443824.2:n.300+20252C>T
|
|
ENST00000544604.6:c.300+20252C>T
|
ENSP00000443824.2:n.300+20252C>T
|
|
NM_001206998.1:c.300+20252C>T
|
NP_001193927.1:n.300+20252C>T
|
|
XM_011530434.1:c.48+19207C>T
|
XP_011528736.1:n.48+19207C>T
|
|
XM_011530435.1:c.15+82139C>T
|
XP_011528737.1:n.15+82139C>T
|
|
XM_011530436.1:c.15+82139C>T
|
XP_011528738.1:n.15+82139C>T
|
|
XM_011530437.1:c.15+82139C>T
|
XP_011528739.1:n.15+82139C>T
|
|
XM_011530438.1:c.15+82139C>T
|
XP_011528740.1:n.15+82139C>T
|
|
XM_011530440.1:c.-1+19288C>T
|
XP_011528742.1:n.-1+19288C>T
|
|
XM_011530435.2:c.15+82139C>T
|
XP_011528737.1:n.15+82139C>T
|
|
XM_011530436.3:c.15+82139C>T
|
XP_011528738.1:n.15+82139C>T
|
|
XM_011530438.2:c.15+82139C>T
|
XP_011528740.1:n.15+82139C>T
|
|
XM_017028990.1:c.15+82139C>T
|
XP_016884479.1:n.15+82139C>T
|
|
NM_001206998.2:c.300+20252C>T
MANE Select
|
NP_001193927.1:n.300+20252C>T
|
|